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(4,5-dibromo-1-methyl-1H-imidazol-2-yl)methanol is a chemical compound with the molecular formula C5H6Br2N2O, derived from the imidazole heterocyclic ring. It features two bromine atoms, a methyl group, and a hydroxymethyl group, which contribute to its antifungal properties by disrupting fungal cell membranes.

881997-90-6

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881997-90-6 Usage

Uses

Used in Antifungal Applications:
(4,5-dibromo-1-methyl-1H-imidazol-2-yl)methanol is used as an antifungal agent for its ability to inhibit fungal growth by disrupting the integrity of fungal cell membranes. The presence of bromine atoms in the molecule enhances its antifungal activity, making it a valuable ingredient in various commercial antifungal products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4,5-dibromo-1-methyl-1H-imidazol-2-yl)methanol is used as an active ingredient in the development of antifungal medications. Its effectiveness against a range of fungi makes it a promising candidate for treating fungal infections.
Used in Agricultural Industry:
(4,5-dibromo-1-methyl-1H-imidazol-2-yl)methanol is also utilized in the agricultural industry as a fungicide to protect crops from fungal diseases, thereby improving crop yield and quality. Its broad-spectrum antifungal action helps in controlling various fungal pathogens that can damage or destroy crops.

Check Digit Verification of cas no

The CAS Registry Mumber 881997-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,9,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 881997-90:
(8*8)+(7*8)+(6*1)+(5*9)+(4*9)+(3*7)+(2*9)+(1*0)=246
246 % 10 = 6
So 881997-90-6 is a valid CAS Registry Number.

881997-90-6Downstream Products

881997-90-6Relevant academic research and scientific papers

Synthesis, crystal structure and antibacterial activity of new highly functionalized ionic compounds based on the imidazole nucleus

Bahnous, Mebarek,Bouraiou, Abdelmalek,Chelghoum, Meryem,Bouacida, Sofiane,Roisnel, Thierry,Smati, Farida,Bentchouala, Chafia,Gros, Philippe C.,Belfaitah, Ali

, p. 1274 - 1278 (2013/03/14)

Several new highly functionalized imidazolium derivatives were synthesized, via appropriate synthetic routes, using imidazole, 1-methylimidazole and 2-phenyl-1-methylimidazole as key intermediates. The antibacterial activity of the prepared compounds was evaluated against: Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Salmonella thipymurium using disk-diffusion and MIC methods. Crystal X-ray structures are reported for six compounds.

Convenient multi-gram scale synthesis of polybrominated imidazoles building blocks

Bahnous, Mebarek,Mouats, Chabane,Fort, Yves,Gros, Philippe C.

, p. 1949 - 1951 (2007/10/03)

The multi-gram scale polybromination of variously substituted imidazoles has been realized using a stoichiometric amount of the Br2-DMF complex. Good yields have been obtained compared to other methods using large amounts of acetic acid-sodium acetate buffer.

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